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Synthesis and Characterization of Co3O4-MnxCo3-xO4 Core-Shell Nanoparticles

Published online by Cambridge University Press:  21 May 2018

Ning Bian ,
Robert A. Mayanovic  and
Mourad Benamara
Ning Bian*
Affiliation:
Department of Physics, Astronomy & Materials Science, Missouri State University, Springfield, MO65897, U.S.A.
Robert A. Mayanovic
Affiliation:
Department of Physics, Astronomy & Materials Science, Missouri State University, Springfield, MO65897, U.S.A.
Mourad Benamara
Affiliation:
Institute for Nanoscience & Engineering, University of Arkansas, Fayetteville, AR72071
*
*(Email: [email protected])
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Abstract

The mixed-valence oxide Co3O4 nanoparticles, having the normal spinel structure, possess large surface area, active-site surface adsorption properties, and fast ion diffusivities. Consequently, they are widely used in lithium-ion batteries, as well as for gas sensing and heterogeneous catalysis applications. In our research, we use a two-step method to synthesize Co3O4–based core-shell nanoparticles (CSNs). Cobalt oxide (Co3O4) nanoparticles were successfully synthesized using a wet synthesis method employing KOH and cobalt acetate. Manganese was incorporated into the Co3O4 structure to synthesize inverted Co3O4@MnxCo3-xO4 CSNs using a hydrothermal method. By adjustment of pH value, we obtained two different morphologies of CSNs, one resulting in pseudo-spherical and octahedron-shaped nanoparticles (PS type) whereas the second type predominantly have a nanoplate (NP type) morphology. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and x-ray photoelectron spectroscopy (XPS) have been performed in order to determine the morphological and structural properties of our CSNs, whereas the magnetic properties have been characterized using a superconducting quantum interference device (SQUID) magnetometer. XRD and TEM results show that the CSNs have the same spinel crystal structure throughout the core and shell with an average particle size of ∼19.8 nm. Our Co3O4 nanoparticles, as measured prior to CSN formation, are shown to be antiferromagnetic (AFM) in nature as shown by the magnetization data. Our SQUID data indicate that the core-shell nanoparticles have both AFM (due to the Co3O4 core) and ferrimagnetic properties (of the shell) with a coercivity field of 300 Oe and 150 Oe at 5 K for the PS and NP samples, respectively. The magnetization vs temperature data show a spin order-disorder transition at ∼33 K and a superparamagnetic blocking temperature of ∼90 K for both batches.

Keywords

hydrothermalmagnetic propertiesnanostructure
Type
Articles
Information
MRS Advances , Volume 3 , Issue 47-48: Nanomaterials , 2018 , pp. 2899 - 2904
Copyright
Copyright © Materials Research Society 2018 

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References

REFERENCES

Cabuil, V., Dupuis, V., Talbot, D., and Neveu, S., J. Magn. Magn. Mater. 323, 1238 (2011).CrossRefGoogle Scholar
Schmidt, W., ChemCatChem 1, 53 (2009).CrossRefGoogle Scholar
Hossain, M.D., Mayanovic, R.A., Sakidja, R., Benamara, M., and Wirth, R., Nanoscale 10, 2138 (2018).CrossRefGoogle Scholar
Lou, X.W., Deng, D., Lee, J.Y., and Archer, L.A., J. Mater. Chem. 18, 4397 (2008).CrossRefGoogle Scholar
Wang, X., Tian, W., Zhai, T., Zhi, C., Bando, Y., and Golberg, D., J. Mater. Chem. 22, 23310 (2012).CrossRefGoogle Scholar
Li, W.Y., Xu, L.N., and Chen, J., Adv. Funct. Mater. 15, 851 (2005).CrossRefGoogle Scholar
Xie, X., Li, Y., Liu, Z.-Q., Haruta, M., and Shen, W., Nature 458, 746 (2009).CrossRefGoogle Scholar
Roth, W.L., J. Phys. 25, 507 (1964).CrossRefGoogle Scholar
Fan, S., Wang, W., Ke, H., Rao, J.-C., and Zhou, Y., RSC Adv. 6, 97055 (2016).CrossRefGoogle Scholar
Chen, Y.H., Zhou, J.F., Mullarkey, D., O’Connell, R., Schmitt, W., Venkatesan, M., Coey, M., and Zhang, H.Z., AIP Adv. 5, 087122 (2015).CrossRefGoogle Scholar
Teng, Y., Song, L.X., Wang, L.B., and Xia, J., J. Phys. Chem. C 118, 4767 (2014).CrossRefGoogle Scholar
Hossain, M.D., Dey, S., Mayanovic, R.A., and Benamara, M., MRS Adv. 1, 2387 (2016).CrossRefGoogle Scholar
Dey, S., Hossain, M.D., Mayanovic, R.A., Wirth, R., and Gordon, R.A., J. Mater. Sci. 52, 2066 (2017).CrossRefGoogle Scholar
Athar, T., Hakeem, A., Topnani, N., and Hashmi, A., Int. Sch. Res. Not. (2012).Google Scholar
Shannon, R.D., Acta Crystallogr. A 32, 751 (1976).CrossRefGoogle Scholar